
$\begin{array}{*{20}{c}}{CHO}\\|\\{HCOH}\\|\\{HOCH}\\|\\{HCOH}\\|\\{C{H_2}OH}\\I\end{array}$ $\begin{array}{*{20}{c}}{CHO}\\|\\{HCOH}\\|\\{HCOH}\\|\\{HOCH}\\|\\{C{H_2}OH}\\{II}\end{array}$ $\begin{array}{*{20}{c}}{CHO}\\|\\{HCOH}\\|\\{HCOH}\\|\\{HCOH}\\|\\{C{H_2}OH}\\{III}\end{array}$
(Given: specific rotations of ($+$)-sucrose, ($+$)-maltose, $L$-($-$)-glucose anc. $+(+)$-fructose in aqueous solution are $+66^{\circ},+140^{\circ},-52^{\circ}$ and $+92^{\circ}$, respectively)
($A$) 'invert sugar' is prepared by acid catalyzed hydrolysis of maltose
($B$) . 'invert sugar' is an equimolar mixture of $D$-($+$)-glucose and $D$-($-$)-fructose
($C$) specific rotation of 'invert sugar' is $-20^{\circ}$
($D$) on reaction with $\mathrm{Br}_2$ water, 'invert sugar' forms saccharic acid as one of the products